Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 Biomarker GENOMICS_ENGLAND Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant. 29388319

2018

Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 Biomarker CLINGEN Deficiency of the Mitochondrial NAD Kinase Causes Stress-Induced Hepatic Steatosis in Mice. 28923496

2018

Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 Biomarker GENOMICS_ENGLAND Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient. 27940755

2016

Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 Biomarker CLINGEN Lysine Restriction and Pyridoxal Phosphate Administration in a NADK2 Patient. 27940755

2016

Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 Biomarker CLINGEN Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia. 24847004

2014

Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 GermlineCausalMutation ORPHANET Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia. 24847004

2014

Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 Biomarker CLINGEN Identification and characterization of a human mitochondrial NAD kinase. 23212377

2012

Entrez Id: 133686
Gene Symbol: NADK2
NADK2
2,4-Dienoyl-CoA Reductase Deficiency
0.600 Biomarker CTD_human